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7/14/2009 5:01:45 PM
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UCREFRP
UCREFRP Catalog Number
7646
Author
Gadomski, D. M. and J. A. Hall-Griswold
Title
Predation by Northern Squawfish on Live and Dead Juvenile Chinook Salmon
USFW Year
1992
USFW - Doc Type
Transactions of the American Fisheries Society
Copyright Material
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<br />682 <br /> <br />NOTES <br /> <br />TABLE I.-Consumption of live and dead juvenile chinook salmon by northern squawfish in six laboratory <br />experiments. Trial results are pooled. Northern squawfish were offered either 50% dead and 50% live or 20% dead <br />and 80% Jive chinook salmon. Two experimental systems were used: 1,400-L circular tanks (CT) with 3 northern <br />squawfish per trial, and an 11,300-L raceway (RW) with 10 northern squawfish per trial. One set of trials was <br />conducted in complete darkness (CT-dark: <0.01 lux); an additional set of trials was in bright light only (CT-light: <br />215-270 lux). All other trials were in a natural photoperiod with both light and dark periods. Degrees of freedom <br />for pooled x2 = 1. Asterisks denote P < 0.05* or P < 0.0 I **. <br /> <br /> Experimental conditions <br />Percen t Prey consumed <br />dead Duration Number Total Percent Pooled <br />salmon System (h) of trials number dead x2 I-{J <br />50 CT 24 18 332 61.8 18.3.. >0.95 <br />50 RW 3 3 132 78.8 43.7.* >0.95 <br />20 CT 24 12 118 35.6 17.9.* >0.95 <br />20 RW 3 3 36 36.1 5.8* >0.75 <br />20 CT -dark 4 22. 79 31.2 6.7** >0.75 <br />20 CT-light 4 22 59 88.1 171.2** >0.95 <br /> <br />· Twenty-seven CT -dark trials were conducted. but only 22 were used in analyses because more than 50% of the available prey <br />were consumed during 5 trials. <br /> <br />consumed (no selection) were I: I (50% dead prey) <br />and 1:4 (20% dead prey). The power (I - (J) of <br />the chi-square tests was computed from formulas <br />in Sokal and Rohlf ( I 981). <br /> <br />Results <br />More than 50% of prey were eaten in only five <br />trials (total N = 85). These trials, which were part <br />of the 4-h dark experiment, were excluded from <br />analysis. <br />All trials with 50% dead prey in the circular <br />tanks and raceway could be validly tested by a <br />heterogeneity chi-square analysis. During 14 of <br />the 18 circular tank trials, 50% or more of the <br />total number of prey consumed were dead. The <br />mean percentage of dead prey consumed was <br />63.6% (SO, 16.7; N = 18). Total (x2 = 53.8; df = <br />18) and pooled (x2 = 18.3; df = I; Table I) data <br />deviated significantly (P < 0.0 I) from the expect- <br />ed frequencies of live and dead prey consumed. <br />Between-trial heterogeneity (x2 = 35.5; df = 17) <br />was also significant (P < 0.0 I); however, this was <br />largely due to the relatively small number of prey <br />consumed per circular tank (mean, 18.4; SO, 5.0; <br />N = 18). The few prey consumed caused many <br />individual tests to have low power (range of I - <br />(j, 0.1-0.9) to detect a small percent change from <br />the expected frequency. In contrast, if data were <br />pooled, the power of the chi-square test exceeded <br />0.95 (Table I). <br />During the raceway trials with 50% dead prey, <br />the mean percentage of dead prey consumed was <br />78.5% (SO, 2.13; N = 3). Total (x2 = 44.0; df = <br />3) and pooled (X2 = 43.7; df = 1; Table 1) data <br />were significantly different (P < 0.01) from ex- <br /> <br />pected frequencies, but in contrast to the circular <br />tank replicates, heterogeneity was not significant <br />(x2 = 0.3; df= 2). Mean number of prey consumed <br />per raceway trial was 44.0 (SO, 9.6; N = 3). The <br />power of individual raceway tests to detect the <br />observed percent change from the expected fre- <br />quency exceeded 0.9. <br />In experiments with 20% dead prey, too few <br />prey were consumed per tank for unbiased chi- <br />square analyses of individual trial results. Mean <br />number of prey consumed per trial during the 24-h <br />circular tank experiment was 9.8 (SO, 3.1; N = <br />12); in the raceway, the mean number of prey <br />consumed was 12.0 (SO, 4.1; N = 3). Therefore, <br />trial results were pooled within each experimental <br />type. Pooled results differed significantly from ex- <br />pected frequencies (Table I). <br />Northern squawfish were much more selective <br />for dead chinook salmon during the light trials <br />than during the dark trials (Table I). During bright <br />light, when 20% dead prey were available, 88.1 % <br />of consumed prey were dead. Periodic counts of <br />uneaten prey during II trials in the light experi- <br />ment indicated that most dead prey were eaten <br />soon after they were placed in the tanks. Twenty- <br />two of 27 dead prey consumed (81.5%) were in- <br />gested within 0.5 h after trials began; 26 of27 dead <br />prey (96.3%) were ingested within 2 h. During the <br />same trials only two live prey were consumed, <br />both within the first 0.5 h. <br />Live prey were occasionally killed by northern <br />squawfish but not ingested. Pharyngeal tooth marks <br />on the sides of these individuals suggested that <br />northern squawfish had attempted to swallow these <br />prey tailfirst and then had regurgitated them. Re- <br />
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